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3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran
In the title compound, C(21)H(21)BrO(3)S, the cyclohexyl ring adopts a chair conformation. The dihedral angle between the mean planes of the benzofuran and 2-bromophenyl fragments is 82.47 (5)°. In the crystal, molecules related by inversion are paired into dimers via C—H⋯π and π–π interactions...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998423/ https://www.ncbi.nlm.nih.gov/pubmed/24765022 http://dx.doi.org/10.1107/S1600536814003547 |
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author | Choi, Hong Dae Seo, Pil Ja Lee, Uk |
author_facet | Choi, Hong Dae Seo, Pil Ja Lee, Uk |
author_sort | Choi, Hong Dae |
collection | PubMed |
description | In the title compound, C(21)H(21)BrO(3)S, the cyclohexyl ring adopts a chair conformation. The dihedral angle between the mean planes of the benzofuran and 2-bromophenyl fragments is 82.47 (5)°. In the crystal, molecules related by inversion are paired into dimers via C—H⋯π and π–π interactions, the latter are indicated by the short distance of 3.607 (3) Å between the centroids of the furan rings. Intermolecular C—H⋯O hydrogen bonds and short Br⋯O [3.280 (1) Å] contacts further consolidate the crystal packing. |
format | Online Article Text |
id | pubmed-3998423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-39984232014-04-24 3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran Choi, Hong Dae Seo, Pil Ja Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(21)BrO(3)S, the cyclohexyl ring adopts a chair conformation. The dihedral angle between the mean planes of the benzofuran and 2-bromophenyl fragments is 82.47 (5)°. In the crystal, molecules related by inversion are paired into dimers via C—H⋯π and π–π interactions, the latter are indicated by the short distance of 3.607 (3) Å between the centroids of the furan rings. Intermolecular C—H⋯O hydrogen bonds and short Br⋯O [3.280 (1) Å] contacts further consolidate the crystal packing. International Union of Crystallography 2014-02-22 /pmc/articles/PMC3998423/ /pubmed/24765022 http://dx.doi.org/10.1107/S1600536814003547 Text en © Choi et al. 2014 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Choi, Hong Dae Seo, Pil Ja Lee, Uk 3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran |
title | 3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran |
title_full | 3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran |
title_fullStr | 3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran |
title_full_unstemmed | 3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran |
title_short | 3-(2-Bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran |
title_sort | 3-(2-bromophenylsulfonyl)-5-cyclohexyl-2-methyl-1-benzofuran |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998423/ https://www.ncbi.nlm.nih.gov/pubmed/24765022 http://dx.doi.org/10.1107/S1600536814003547 |
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